Method for preparing Rhodiola rosea solid-state transformation fermentate by using microbial mixing bacterial strain
A technology of mixed strains and rhodiola, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., to achieve the effect of reducing the consumption of raw medicinal materials
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0033] This embodiment is the preparation of Aspergillus niger and Aspergillus oryzae mycelia.
[0034] 1) Mash the natural wild Rhodiola rosea medicinal material, take 1g, add 5ml of sterile water, shake well, and then dilute 10, 100, 1000 and 10000 times with sterile water respectively. Take 0.1ml of each of the above dilutions, spread them on the separation medium consisting of 10g of glucose, 5g of peptone, 5g of yeast extract, 1g of potassium dihydrogen phosphate, 0.5g of ammonium sulfate, 20g of agar and 1000ml of water. Cultivate for 3 days, pick a single colony, and select a bacterial strain whose content of salidroside is increased after being transformed and fermented in the Rhodiola rosea medium and detected by high performance liquid chromatography (HPLC).
[0035] 2) Mix Rhodiola rosea powder, bran and water with a particle size of 80 mesh at 0.8:0.2:1 by weight, and then steam sterilize to obtain the Rhodiola rosea bran seed culture medium, and then inoculate them ...
Embodiment 2
[0037] Crush 100g of Rhodiola rhizome raw materials to 80 mesh, then add 0.05g of yeast extract, 0.05g of potassium dihydrogen phosphate, 0.02g of magnesium sulfate and 100mL of water, stir and mix evenly to make it a solid culture material for Rhodiola rosea, and use steam Sterilize at 121 DEG C for 30 minutes; After cooling, inoculate the mixed mold mycelium of 5g (wet weight) prepared by the method of Example 1, wherein the weight ratio of Aspergillus niger (Aspergillus niger) and Aspergillus oryzae (Aspergillus oryzae) is 8:2, and then incubated and fermented at 28°C for 60 hours.
[0038] The obtained solid transformation fermented product is detected by high performance liquid chromatography (HPLC), and the content of salidroside is 1.1869%. Compared with the salidroside content of the original medicinal material detected under the same conditions as 0.7306%, the converted fermented product The content of salidroside can be increased by 62.46%.
Embodiment 3
[0040] Crush 100g of Rhodiola rhizome raw materials to 80 mesh, then add 0.1g of yeast extract, 0.1g of potassium dihydrogen phosphate, 0.03g of magnesium sulfate and 100mL of water, stir and mix evenly to make it a solid culture material for Rhodiola rosea, and use steam Sterilize at 121 DEG C for 30 minutes; After cooling, inoculate the mixed mold mycelium of 7.5g (wet weight) prepared by the method of Example 1, wherein the weight ratio of Aspergillus niger (Aspergillus niger) and Aspergillus oryzae (Aspergillus oryzae) 6:4, and then incubated and fermented at 30°C for 55 hours.
[0041] The obtained solid transformation fermented product is detected by high performance liquid chromatography (HPLC), and the salidroside content is 1.2469%. Compared with the salidroside content of the original medicinal material detected under the same conditions as 0.7306%, the converted fermented product The content of salidroside can be increased by 70.67%.
PUM
| Property | Measurement | Unit |
|---|---|---|
| Particle size | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 